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Sphingolipid signaling pathways have been implicated in many critical cellular events. Sphingosine-1-phosphate (SPP), a sphingolipid metabolite found in high concentrations in platelets and blood, stimulates members of the endothelial differentiation gene (Edg) family of G protein-coupled receptors and triggers diverse effects, including cell growth, survival, migration, and morphogenesis. To determine the in vivo functions of the SPP/Edg signaling pathway, we disrupted the Edg1 gene in mice. Edg1(-/-) mice exhibited embryonic hemorrhage leading to intrauterine death between E12.5 and E14.5. Vasculogenesis and angiogenesis appeared normal in the mutant embryos. However, vascular maturation was incomplete due to a deficiency of vascular smooth muscle cells/pericytes. We also show that Edg-1 mediates an SPP-induced migration response that is defective in mutant cells due to an inability to activate the small GTPase, Rac. Our data reveal Edg-1 to be the first G protein-coupled receptor required for blood vessel formation and show that sphingolipid signaling is essential during mammalian development.
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Yujing Liu
Lanzhou University
Ryuichi Wada
Sendai Kousei Hospital
Tadashi Yamashita
Azabu University
Journal of Clinical Investigation
National Institutes of Health
Georgetown University
National Institute of Diabetes and Digestive and Kidney Diseases
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Liu et al. (Sun,) studied this question.
synapsesocial.com/papers/6a22009e1b095894fc4eac2a — DOI: https://doi.org/10.1172/jci10905
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